Haustrate Aurélien, Shapovalov George, Spriet Corentin, Cordier Clément, Kondratskyi Artem, Noyer Lucile, Foulquier François, Prevarskaya Natalia, Lehen'kyi V'yacheslav
Laboratory of Cell Physiology, INSERM U1003, Laboratory of Excellence Ion Channels Science and Therapeutics, Department of Biology, Faculty of Science and Technologies, University of Lille, 59650 Villeneuve d'Ascq, France.
FONDATION ARC, 9 rue Guy Môquet, 94830 Villejuif, France.
Cancers (Basel). 2023 Mar 17;15(6):1825. doi: 10.3390/cancers15061825.
The TRPV6 calcium channel is known to be up-regulated in various tumors. The efforts to target the TRPV6 channel in vivo are still ongoing to propose an effective therapy against cancer. Here, we report the generation of two antibodies raised against extracellular epitopes corresponding to the extracellular loop between S1 and S2 (rb79) and the pore region (rb82). These antibodies generated a complex biphasic response with the transient activation of the TRPV6 channel. Store-operated calcium entry was consequently potentiated in the prostate cancer cell line LNCaP upon the treatment. Both rb79 and rb82 antibodies significantly decreased cell survival rate in a dose-dependent manner as compared to the control antibodies of the same isotype. This decrease was due to the enhanced cell death via apoptosis revealed using a sub-G1 peak in a cell cycle assay, TUNEL assay, and a Hoechst staining, having no effects in the PC3M cell line. Moreover, all TUNEL-positive cells had TRPV6 membrane staining as compared to the control antibody treatment where TRPV6-positive cells were all TUNEL negative. These data clearly demonstrate that TRPV6 channel targeting using rb79 and rb82 antibodies is fatal and may be successfully used in the anticancer therapies.
已知瞬时受体电位香草酸亚型6(TRPV6)钙通道在多种肿瘤中上调。针对TRPV6通道进行体内靶向治疗的研究仍在进行中,旨在提出一种有效的抗癌疗法。在此,我们报告了两种针对细胞外表位产生的抗体,它们分别对应于S1和S2之间的细胞外环(rb79)以及孔区域(rb82)。这些抗体对TRPV6通道的瞬时激活产生了复杂的双相反应。因此,在前列腺癌细胞系LNCaP中,处理后储存-操作性钙内流增强。与相同亚型的对照抗体相比,rb79和rb82抗体均以剂量依赖的方式显著降低细胞存活率。这种降低是由于通过细胞周期分析中的亚G1峰、末端脱氧核苷酸转移酶介导的缺口末端标记(TUNEL)分析和Hoechst染色显示的凋亡导致细胞死亡增加,而在PC3M细胞系中没有影响。此外,与对照抗体处理相比,所有TUNEL阳性细胞均有TRPV6膜染色,在对照抗体处理中TRPV6阳性细胞均为TUNEL阴性。这些数据清楚地表明,使用rb79和rb82抗体靶向TRPV6通道是致命的,可能成功用于抗癌治疗。